Tissue-directed antibodies and methods of using the same
US-2024342260-A1 · Oct 17, 2024 · US
US2016304608A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016304608-A1 |
| Application number | US-201615139784-A |
| Country | US |
| Kind code | A1 |
| Filing date | Apr 27, 2016 |
| Priority date | Jun 2, 2011 |
| Publication date | Oct 20, 2016 |
| Grant date | — |
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The disclosure relates to antibodies that bind FcRn and methods of using these antibodies.
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1 - 44 . (canceled) 45 : A kit comprising: an FcRn-binding antibody comprising a light chain variable region (V L ), a heavy chain variable region (V H ), and a heavy chain constant region (C H ), wherein the V L of the antibody comprises: (i) a V L CDR1 comprising the amino acid sequence TGTGSDVGSYNLVS (SEQ ID NO: 14); (ii) a V L CDR2 comprising the amino acid sequence GDSQRPS (SEQ ID NO: 15); and (iii) a V L CDR3 comprising the amino acid sequence CSYAGSGIYV (SEQ ID NO: 25), SSYAGSGIYV (SEQ ID NO: 12) or ASYAGSGIYV (SEQ ID NO: 13); and the V H of the antibody comprises: (i) a V H CDR1 comprising the amino acid sequence EYAMG (SEQ ID NO: 22); (ii) a V H CDR2 comprising the amino acid sequence SIGSSGGQTKYADSVKG (SEQ ID NO: 23); and (iii) a V H CDR3 comprising the amino acid sequence LAIGDSY (SEQ ID NO: 24); and the C H of the antibody has a deletion corresponding to the C-terminal lysine residue at the last position of SEQ ID NO: 17, and further comprising informational material. 46 : The kit of claim 45 , wherein the informational material is selected from the group consisting of: information about production of the compound, molecular weight of the compound, concentration, date of expiration, and batch or production site information. 47 : The kit of claim 45 , wherein the informational material comprises instructions to administer the FcRn-binding antibody in a suitable manner. 48 : The kit of claim 45 , wherein the FcRn-binding antibody is a part of a composition. 49 : The kit of claim 48 , wherein the composition further comprises an ingredient selected from the group consisting of: a solvent or buffer, a stabilizer, a preservative, a flavoring agent, a fragrance or other cosmetic ingredient, and a second agent for treating an autoimmune disorder. 50 : The kit of claim 45 , further comprising one or more containers for the composition containing the FcRn antibody. 51 : A method of removing an unwanted therapeutic antibody from the bloodstream, comprising administering an FcRn-binding antibody to a subject, wherein the antibody comprises a light chain variable region (V L ), a heavy chain variable region (V H ), and a heavy chain constant region (C H ), wherein the V L of the antibody comprises: (i) a V L CDR1 comprising the amino acid sequence TGTGSDVGSYNLVS (SEQ ID NO: 14); (ii) a V L CDR2 comprising the amino acid sequence GDSQRPS (SEQ ID NO: 15); and (iii) a V L CDR3 comprising the amino acid sequence CSYAGSGIYV (SEQ ID NO: 25), SSYAGSGIYV (SEQ ID NO: 12) or ASYAGSGIYV (SEQ ID NO: 13); and the V H of the antibody comprises: (i) a V H CDR1 comprising the amino acid sequence EYAMG (SEQ ID NO:22); (ii) a V H CDR2 comprising the amino acid sequence SIGSSGGQTKYADSVKG (SEQ ID NO: 23); and (iii) a V H CDR3 comprising the amino acid sequence LAIGDSY (SEQ ID NO: 24); and the C H of the antibody has a deletion corresponding to the C-terminal lysine residue at the last position of SEQ ID NO: 17. 52 : A method of suppressing a level of anti-Human Leukocyte Antigens (HLA), comprising administering an FcRn-binding antibody to a subject, wherein the antibody comprises a light chain variable region (V L ), a heavy chain variable region (V H ), and a heavy chain constant region (C H ), wherein the V L of the antibody comprises: (i) a V L CDR1 comprising the amino acid sequence TGTGSDVGSYNLVS (SEQ ID NO: 14); (ii) a V L CDR2 comprising the amino acid sequence GDSQRPS (SEQ ID NO: 15); and (iii) a V L CDR3 comprising the amino acid sequence CSYAGSGIYV (SEQ ID NO: 25), SSYAGSGIYV (SEQ ID NO: 12) or ASYAGSGIYV (SEQ ID NO: 13); and the V H of the antibody comprises: (i) a V H CDR1 comprising the amino acid sequence EYAMG (SEQ ID NO: 22); (ii) a V H CDR2 comprising the amino acid sequence SIGSSGGQTKYADSVKG (SEQ ID NO: 23); and (iii) a V H CDR3 comprising the amino acid sequence LAIGDSY (SEQ ID NO: 24); and the C H of the antibody has a deletion corresponding to the C-terminal lysine residue at the last position of SEQ ID NO: 17. 53 : The method of claim 52 , wherein the antibody is administered in connection with organ transplant. 54 : A method for delivering macro and/or micromolecules into a cell, comprising contacting an FcRn-binding antibody to the cell, wherein the antibody comprises a light chain variable region (V L ), a heavy chain variable region (V H ), and a heavy chain constant region (C H ), wherein the V L of the antibody comprises: (i) a V L CDR1 comprising the amino acid sequence TGTGSDVGSYNLVS (SEQ ID NO: 14); (ii) a V L CDR2 comprising the amino acid sequence GDSQRPS (SEQ ID NO: 15); and (iii) a V L CDR3 comprising the amino acid sequence CSYAGSGIYV (SEQ ID NO: 25), SSYAGSGIYV (SEQ ID NO: 12) or ASYAGSGIYV (SEQ ID NO: 13); and the V H of the antibody comprises: (i) a V H CDR1 comprising the amino acid sequence EYAMG (SEQ ID NO: 22); (ii) a V H CDR2 comprising the amino acid sequence SIGSSGGQTKYADSVKG (SEQ ID NO: 23); and (iii) a V H CDR3 comprising the amino acid sequence LAIGDSY (SEQ ID NO: 24); and the C H of the antibody has a deletion corresponding to the C-terminal lysine residue at the last position of SEQ ID NO: 17. 55 : The method of claim 54 , wherein the antibody is administered in connection with gene therapy.
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